反応式
[NH2:1][C:2]1[CH:3]=[C:4]([CH:9]=[CH:10][CH:11]=1)[C:5]([NH:7][NH2:8])=[O:6].C(N(CC)CC)C.[C:19](=S)=[S:20]>C(O)C>[NH2:1][C:2]1[CH:3]=[C:4]([C:5]2[O:6][C:19]([SH:20])=[N:8][N:7]=2)[CH:9]=[CH:10][CH:11]=1参加物
5
実験手順
3-Aminobenzhydrazide (5.76 g) was dissolved in ethanol (40 mL), and triethylamine (4.8 mL) and carbon disulfide (2.1 mL) were added to the solution. The mixture was heated under reflux for 4 hrs. The solvent was evaporated, and water was added. The precipitated solids were collected by filtration to give the title compound (5.06 g) as a pale-yellow powder.
後処理
- temperatureThe mixture was heated
- temperatureunder reflux for 4 hrs
- customThe solvent was evaporated
- additionwater was added
- filtrationThe precipitated solids were collected by filtration
出典と根拠
- ORDレコード
- ord-2272d54bcda141169e47c2ffb68a7bea
- 出典データセット
- uspto-grants-2006_10
- 特許番号
- US07115635B2
関連ノート
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